Juberg-Hayward syndrome: Report of a new patient with severe phenotype and novel clinical features

American Journal of Medical Genetics

Volumn 122 A, Issue 3, 2003, Pages 257-260

  Hedera, Peter ^a,b   Innis, Jeffrey W ^a,c  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b VANDERBILT UNIVERSITY   (United States)

^c Box 0618 ^*  (United States)

Author keywords

Malpuech syndrome; Multiple congenital anomalies; Orofaciodigital syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CLEFT LIP; CLEFT PALATE; CLINICAL FEATURE; CONGENITAL MALFORMATION; DANDY WALKER SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; JUBERG HAYWARD SYNDROME; KARYOTYPE; MALE; MALPUECH SYNDROME; MENTAL DEFICIENCY; METACARPAL BONE; MICROCEPHALY; PHENOTYPE; PRIORITY JOURNAL; RADIOULNAR JOINT; SKELETON MALFORMATION; SYNDROME; SYNOSTOSIS; THUMB MALFORMATION; TONGUE DISEASE; UROGENITAL TRACT MALFORMATION;

EID: 0141857858     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20263     Document Type: Article

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